72850-53-4

Basic information

• Product Name: ETHYL 2-OXO-4-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE
• Synonyms: ETHYL 2-OXO-4-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE;Ethyl 2,3-dihydro-2-oxo-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate
• CAS NO: 72850-53-4
• Molecular Formula: C₇H₆F₃NO₃S
• Molecular Weight: 241.19
• Mol File: 72850-53-4.mol
• Article Data: 3

Chemical Properties

• Melting Point: 122-124°C
• Boiling Point: 346.7°C at 760 mmHg
• Flash Point: 163.5°C
• Appearance: /
• Density: 1.534g/cm³
• Vapor Pressure: 2.82E-05mmHg at 25°C
• Refractive Index: 1.489
• CAS DataBase Reference: ETHYL 2-OXO-4-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2-OXO-4-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE(72850-53-4)
• EPA Substance Registry System: ETHYL 2-OXO-4-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE(72850-53-4)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 72850-53-4(Hazardous Substances Data)

Usage

General Description

ETHYL 2-OXO-4-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE is a specialized chemical compound characterized by its use in various complex reactions in advanced chemistry. It contains elements like sulfur and fluorine, indicated by the terms 'trifluoromethyl' and 'thiazole' in its name. As a type of carboxylate, it has a COOH group, but the hydrogen is replaced by an ethyl group. The '2,3-dihydro' suggests the substance contains a part which is a cyclic compound with two hydrogen atoms. The 'oxo' component identifies the presence of a carbonyl group. Often used in research and development laboratories, this chemical plays a critical role in multiple syntheses and experiments, but little information regarding its properties or uses in a wider context is usually available due to its specific, niche applications.

InChI:InChI=1/C7H6F3NO3S/c1-2-14-5(12)3-4(7(8,9)10)11-6(13)15-3/h2H2,1H3,(H,11,13)

Upstream product

• 141860-78-8 ethyl 3-amino-4,4,4-trifluorocrotonate 
• 2757-23-5 chloro(chlorosulfanyl)methanone 
• 372-29-2 ethyl 3-amino-4,4,4-trifluoro-2-butenoate 

Downstream Products

• 120647-15-6 Ethyl [2,3-dihydro-2-oxo-3-benzyl-4-trifluoromethylthiazol-5-yl]-carboxylate 
• 72850-52-3 ethyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate 
• 72850-80-7 Ethyl 2-fluoro-4-(trifluoromethyl)-5-thiazolecarboxylate 
• 72850-71-6 Methyl-2-chlor-4-trifluormethyl-5-thiazolcarboxylat 
• 72850-61-4 2-chloro-4-(trifluoromethyl)-5-thiazolecarboxylic acid 
• 78451-00-0 2-Chloro-5-<(benzyloxy)methyl>-4-(trifluoromethyl)thiazole 
• 106203-24-1 4-trifluoromethyl-thiazole-5-carboxylic acid ethyl ester 
• 78450-97-2 2-Chloro-4-(trifluoromethyl)-5-thiazolemethanol 
• 72850-81-8 Ethyl 2-phenoxy-4-(trifluoromethyl)-5-thiazolecarboxylate 
• 72860-48-1 2-chloro-4-trifluoromethyl-thiazole-5-carboxylic acid 4-chloro-phenyl ester 
• 72850-64-7 benzyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate 
• 72850-69-2 2-chloro-4-trifluoromethyl-thiazole-5-carboxylic acid phenyl ester 

Relevant articles and documents

Synthesis and biological activity of novel 2-(3-trifluoromethylphenoxy)-4-trifluoromethylthiazole-5-carboxamide derivatives

Novel 2-(3-trifluoromethylphenoxy)-4-trifluoromethylthiazole-5-carboxamides were designed and synthesized utilizing ethyl 3-amino-4,4,4-trifluoro-2-butenoate as a starting material via six steps. Subsequently, their biological activities were evaluated in

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